WATER BATH
K-Number: K822564 · 1982-09-14
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Device Summary
Frequently Asked Questions
What is the WATER BATH?
WATER BATH is a medical device that received FDA 510(k) clearance on 1982-09-14. The listed applicant is Boekel Industries, Inc.. The 510(k) number is K822564.
When did WATER BATH receive FDA 510(k) clearance?
WATER BATH received FDA 510(k) clearance on 1982-09-14, under 510(k) number K822564.
Who is the listed applicant for WATER BATH?
The FDA 510(k) record lists Boekel Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WATER BATH?
The FDA product code for WATER BATH is JTQ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Boekel Industries, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JTQ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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